Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP86721.RAd5pHPIzvJKjYbxt7nGqPGVrGKjWyokM5rkvA-Hd0Hn4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP86721.RAd5pHPIzvJKjYbxt7nGqPGVrGKjWyokM5rkvA-Hd0Hn4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP86721.RAd5pHPIzvJKjYbxt7nGqPGVrGKjWyokM5rkvA-Hd0Hn4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP86721.RAd5pHPIzvJKjYbxt7nGqPGVrGKjWyokM5rkvA-Hd0Hn4130_provenance.
- NP86721.RAd5pHPIzvJKjYbxt7nGqPGVrGKjWyokM5rkvA-Hd0Hn4130_assertion description "[No association between FD and the genotype of the insertion/deletion polymorphism in the promoter of SERT (SERT-P) or HTR3A C178T polymorphism was observed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86721.RAd5pHPIzvJKjYbxt7nGqPGVrGKjWyokM5rkvA-Hd0Hn4130_provenance.
- NP86721.RAd5pHPIzvJKjYbxt7nGqPGVrGKjWyokM5rkvA-Hd0Hn4130_assertion evidence source_evidence_literature NP86721.RAd5pHPIzvJKjYbxt7nGqPGVrGKjWyokM5rkvA-Hd0Hn4130_provenance.
- NP86721.RAd5pHPIzvJKjYbxt7nGqPGVrGKjWyokM5rkvA-Hd0Hn4130_assertion SIO_000772 18331431 NP86721.RAd5pHPIzvJKjYbxt7nGqPGVrGKjWyokM5rkvA-Hd0Hn4130_provenance.
- NP86721.RAd5pHPIzvJKjYbxt7nGqPGVrGKjWyokM5rkvA-Hd0Hn4130_assertion wasDerivedFrom gad-20130706 NP86721.RAd5pHPIzvJKjYbxt7nGqPGVrGKjWyokM5rkvA-Hd0Hn4130_provenance.
- NP86721.RAd5pHPIzvJKjYbxt7nGqPGVrGKjWyokM5rkvA-Hd0Hn4130_assertion wasGeneratedBy ECO_0000203 NP86721.RAd5pHPIzvJKjYbxt7nGqPGVrGKjWyokM5rkvA-Hd0Hn4130_provenance.
- gad-20130706 importedOn "2013-07-06" NP86721.RAd5pHPIzvJKjYbxt7nGqPGVrGKjWyokM5rkvA-Hd0Hn4130_provenance.